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The Minor "A" allele is associated with:

  • Increased risk of Crohn's disease [R].

This SNP is associated with (unknown alleles):

  • associated with levels of vitamin B(12) in Indian population  [R]

rs602662

Parent Gene: FUT2

Importance: 3
Less common allele: A = 33%
More common allele: G = 67%
My Genotype: Log In
Risk Allele: A, G, A

Disease/Trait: Vitamin B12 Measurement

The A allele of rs602662 is reported to be associated with Vitamin B12 Measurement (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Vitamin B12 levels.

Disease/Trait: Systemic Lupus Erythematosus

The G allele of rs602662 is reported to be associated with Systemic Lupus Erythematosus (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Autoimmune Disease

The G allele of rs602662 is reported to be associated with Autoimmune Disease (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Crohn's Disease

The G allele of rs602662 is reported to be associated with Crohn's Disease (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Ulcerative Colitis

The G allele of rs602662 is reported to be associated with Ulcerative Colitis (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Celiac Disease

The G allele of rs602662 is reported to be associated with Celiac Disease (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Psoriasis

The G allele of rs602662 is reported to be associated with Psoriasis (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Ankylosing Spondylitis

The G allele of rs602662 is reported to be associated with Ankylosing Spondylitis (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Chronic Childhood Arthritis

The G allele of rs602662 is reported to be associated with Chronic Childhood Arthritis (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Common Variable Immunodeficiency

The G allele of rs602662 is reported to be associated with Common Variable Immunodeficiency (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Type I Diabetes Mellitus

The G allele of rs602662 is reported to be associated with Type I Diabetes Mellitus (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Autoimmune Thyroid Disease

The G allele of rs602662 is reported to be associated with Autoimmune Thyroid Disease (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Pediatric autoimmune diseases.

Disease/Trait: Vitamin B12 Measurement

rs602662 is associated with Vitamin B12 Measurement (R). It is reported to have a 0.07 unit decrease on Folate pathway vitamin levels (Plasma Vitamin B12). No specific risk allele was identified in the study.

Disease/Trait: Vitamin B12 Measurement

The A allele of rs602662 is reported to be associated with Vitamin B12 Measurement (R). Your genotype was not identified for this SNP so we are unable to comment on your association with Folate pathway vitamin levels (vitamin B12).